CN104882600A - Preparation method for iron oxide microspheres as negative electrode material of lithium ion battery - Google Patents
Preparation method for iron oxide microspheres as negative electrode material of lithium ion battery Download PDFInfo
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- CN104882600A CN104882600A CN201510150087.5A CN201510150087A CN104882600A CN 104882600 A CN104882600 A CN 104882600A CN 201510150087 A CN201510150087 A CN 201510150087A CN 104882600 A CN104882600 A CN 104882600A
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
- H01M4/622—Binders being polymers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Abstract
The invention discloses a preparation method for iron oxide microspheres as the negative electrode material of a lithium ion battery, which comprises the steps of 1) dissolving the ferric salt in de-ionized water to obtain a ferric salt solution; 2) adding acid in the ferric salt solution obtained in the step 1), then adding PVP in the solution and stirring the solution till the PVP is completely dissolved; 3) adding methanamide while vigorously stirring the solution, and then aging the solution at 50 to 70 DEG C for 2 to 3 hours to obtain a gel; 4) drying the gel at 50 to 70 DEG C for 24 hours under the normal pressure to obtain a precursor product; 5) heating the precursor product obtained in the step 4) in the air atmosphere to about 500 to 800 DEG C, then thermally preserving the product for 4 to 6 hours, and cooling the product to the room temperature to obtain iron oxide microspheres as the negative electrode material. By the above method, the volume expansion problem of Fe2O3 during the charging/discharging process can be solved.
Description
Technical field
The invention belongs to electrochemical field, be specifically related to a kind of preparation method of iron oxide microballoon negative material of lithium ion battery.
Background technology
Lithium ion battery has the advantages such as high voltage, high-energy, long service life, environmental protection, is therefore widely used in the fields such as portable electric appts, electric automobile, Aero-Space.Along with the development of society, conventional carbon negative material is because of its less theoretical specific capacity (372mAh g
-1) and be more and more difficult to the needs meeting reality.The electrode material of exploitation height ratio capacity, high-energy-density becomes the current difficult problem faced.
In recent years, transition metal oxide, as Fe
2o
3, Fe
4o
3, Co
3o
4, CuO, NiO etc., because of it, there is higher theoretical specific capacity and good security performance receives increasing concern.Wherein, Fe
2o
3as the theoretical specific capacity of lithium ion battery negative material close to 3 times of conventional carbon negative material, 1008mAh g can be reached
-1.In addition, Fe
2o
3also having the advantages such as with low cost, raw material sources is abundant, safety and environmental protection, is the very potential high performance lithium ionic cell cathode material of one.But the same with other transition metal oxides, Fe
2o
3the problems such as material exists larger change in volume at charge and discharge process, thus occurs structure collapses, causes the decay of capacity, cyclical stability difference.At present, people are for raising Fe
2o
3much research has been done in material structure stability aspect.Wherein synthesis has micro-nano porous structure material is an effective method, this material effectively can alleviate the volumetric expansion problem of material at charge and discharge process, this structure generally all has certain meso pore characteristics on the other hand, effective increasing specific surface area, increase the contact area of electrolyte and electrode material, thus enhancing electrochemical reaction, effectively improve the cycle performance of material.
For Fe
2o
3the preparation of material mainly contains hydro thermal method, solid phase method and template.Adopt sol gel legal system for Fe
2o
3the report of material is also fewer, although application number be 201210486059.7 domesticly patent reports a kind of preparation method by sol-gal process synthesizing lithium ion battery iron oxide cathode material, but it adopts the mixed solution of alcohol and water as solvent, add the difficulty controlling reaction condition; That is, the more difficult control of reaction condition, technique is more complicated, and its gained pattern does not illustrate.Pure Fe in addition prepared by it
2o
3material is at 0.1A g
-1current density under circulation 20 times after reversible capacity only have 454.8mAh g
-1.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of preparation method of lithium ion battery iron oxide microballoon negative material, adopts method of the present invention to solve Fe
2o
3material is in the volumetric expansion problem of charge and discharge process.
In order to solve the problems of the technologies described above, the invention provides a kind of preparation method of lithium ion battery iron oxide microballoon negative material, comprising the following steps:
1), by iron salt dissolved in deionized water, iron salt solutions (for orange solution) is obtained; Described deionized water and Fe
3+mol ratio be 50 ~ 80:1 (that is, deionized water/Fe
3+=50 ~ 80:1, is preferably 50 ~ 70:1);
2), to step 1) add acid, described acid and Fe in the iron salt solutions of gained
3+mol ratio be 0.3 ~ 1.0:1 (being preferably 0.3 ~ 0.7:1); Then add polyvinylpyrrolidone (PVP) to stir, until polyvinylpyrrolidone dissolves completely; Described polyvinylpyrrolidone and Fe
3+mol ratio be 0.005 ~ 0.015:1 (being preferably 0.007 ~ 0.013:1);
Remarks illustrate: polyvinylpyrrolidonemolecules molecules amount is 10000 ~ 130000;
3), with vigorous stirring add formamide, stir 5 ~ 10 minutes, described formamide and Fe
3+mol ratio be 4 ~ 10:1 (being preferably 4.4 ~ 6.6:1);
Then under 50 ~ 70 DEG C (being preferably 60 DEG C), aged gel is carried out; The aged gel time is 2 ~ 3 hours;
4), by step 3) gel of gained under normal pressure 50 ~ 70 DEG C (being preferably 60 DEG C) dry 24 hours, obtain precursor product;
5), by step 4) precursor product of gained is warming up to 500 ~ 800 DEG C of insulations 4 ~ 6 hours in air atmosphere, and be cooled to room temperature, obtain lithium ion battery iron oxide microballoon negative material (powder shaped).
Improvement as the preparation method of lithium ion battery iron oxide microballoon negative material of the present invention: described molysite is high iron chloride; Described acid is hydrochloric acid.
Further improvement as the preparation method of lithium ion battery iron oxide microballoon negative material of the present invention: deionized water and Fe
3+mol ratio be 50 ~ 60:1, hydrochloric acid and Fe
3+mol ratio be 0.3 ~ 0.4:1, polyvinylpyrrolidone and Fe
3+mol ratio be 0.007 ~ 0.008:1; Formamide and Fe
3+mol ratio be 5.5:1; Step 5) in: be warming up to 500 DEG C of insulations 4 hours.
In the present invention, the speed of stirring is 600 ~ 800r/min, and the speed of vigorous stirring is 800 ~ 1000r/min.
The present invention is that one prepares iron oxide presoma xerogel by sol-gel process and constant pressure and dry, by Technology for Heating Processing, and preparation iron oxide cathode material.
The present invention first adopts gentle sol-gal process synthetic iron oxide presoma block product xerogel, after heat-treat at ambient pressure and obtain iron oxide cathode material.The invention has the advantages that preparation method is simple, mild condition, with low cost, be convenient to large-scale production.The iron oxide microballoon negative material obtained has excellent cycle performance.
The present invention controls gel and phase separation by regulating the consumption of acid (hydrochloric acid) and PVP, finally obtains the iron oxide microballoon with micro-/micro-nano structure, and has certain meso-hole structure.This key issue with the iron oxide microballoon of micro-/micro-nano structure be phase separation agent and gel promoter On The Choice and between the control problem of Degree of interaction, hydrochloric acid is selected to be gel promoter in the present invention, employing polyvinylpyrrolidone is the derivant that is separated, and regulates proportion relation between the two to obtain the iron oxide microballoon with micro-/micro-nano structure.
The present invention adopts single deionized water as solvent, by sol gel method synthesis Fe
2o
3microballoon (uniform micron ball), reaction condition (processing step is simple) simple and easy to control, for lithium ion battery negative material, it is at 0.1A g
-1current density under circulation 100 times after reversible capacity can reach 550mAh g
-1, show excellent cycle performance.
Accompanying drawing explanation
Below in conjunction with accompanying drawing, the specific embodiment of the present invention is described in further detail.
Fig. 1 is the XRD figure of iron oxide microballoon negative material prepared by embodiment 1.
Fig. 2 is 45000 times of stereoscan photographs of iron oxide microballoon negative material prepared by embodiment 1.
Fig. 3 is the cycle performance figure of iron oxide microballoon negative material prepared by embodiment 1.
Fig. 4 is the first charge-discharge curve of iron oxide microballoon negative material prepared by embodiment 1.
Fig. 5 is the cycle performance figure of iron oxide microballoon negative material prepared by embodiment 2.
Fig. 6 is the first charge-discharge curve of iron oxide microballoon negative material prepared by embodiment 2.
Embodiment
In following case, the speed of stirring is 600 ~ 800r/min, and the speed of vigorous stirring is 800 ~ 1000r/min; Polyvinylpyrrolidonemolecules molecules amount is 10000 ~ 130000;
The preparation method of embodiment 1, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.0027mol (about 0.1 milliliter) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2.5 milliliters of formamides (0.044mol) more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative material (powder).
Test 1, iron oxide material--iron oxide microballoon negative material, acetylene black and PVDF (Kynoar) are that 8:1:1 mixes with mass ratio by obtained, be dispersed in (described NMP is 20-39 times of above-mentioned 3 weight sums) in NMP (1-METHYLPYRROLIDONE); Make slurry, evenly be coated on Copper Foil, circular electrode pole piece (coating layer thickness is 0.1-0.5mm) is stamped into after vacuum drying, be to electrode with metal lithium sheet, 1mol/L LiPF6/DMC+EC (volume ratio is 1:1) is electrolyte, Celgard 2300 is barrier film, is assembled into button cell and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 550mAh g
-1, its first discharge capacity be 1295mAhg
-1, charging capacity is 895mAh g
-1.
The preparation method of embodiment 2, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 10 milliliters of (0.555mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add hydrochloric acid 0.0027mol (about 0.1 milliliter) in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2.5 milliliters of (0.044mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 225mAh g
-1, its first discharge capacity be 1085mAh g
-1, charging capacity is 746mAh g
-1.
The preparation method of embodiment 3, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.0054mol (about 0.2 milliliter) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2.5 milliliters of (0.044mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 330mAh g
-1, its first discharge capacity be 1126mAh g
-1, charging capacity is 823mAh g
-1.
The preparation method of embodiment 4, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.0027mol (about 0.1 milliliter) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 1 gram of (0.0001mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2.5 milliliters of (0.044mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 208mAh g
-1, its first discharge capacity be 1054mAh g
-1, charging capacity is 726mAh g
-1.
The preparation method of embodiment 5, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.1 milliliter of (0.0027mol) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2 milliliters of (0.0352mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 425mAh g
-1, its first discharge capacity be 1285mAh g
-1, charging capacity is 825mAh g
-1.
The preparation method of embodiment 6, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.0027mol (about 0.1 milliliter) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 3 milliliters of (0.0528mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 500 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 178mAh g
-1, its first discharge capacity be 985mAh g
-1, charging capacity is 616mAh g
-1.
The preparation method of embodiment 7, a kind of lithium ion battery iron oxide microballoon negative material, carries out following steps successively:
1), take 2.1624 grams of (0.008mol) high iron chloride, be dissolved in 8 milliliters of (0.444mol) deionized waters, stir formation orange solution;
2), under agitation, to step 1) add 0.0027mol (about 0.1 milliliter) hydrochloric acid in gained iron salt solutions, uniform stirring 5 minutes, after add 0.6 gram of (0.00006mol) polyvinylpyrrolidone and be stirred to it and dissolve completely, add 2.5 milliliters of (0.044mol) formamides more with vigorous stirring, stir after 5 minutes, at 60 DEG C, carry out aged gel 3 hours;
3), within 24 hours, precursor product is obtained by dry at normal pressure 60 DEG C for gained gel;
4), by the precursor product of gained be warming up to 800 DEG C of insulations 4 hours in air atmosphere, be cooled to room temperature, obtain iron oxide microballoon negative electrode material powder.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test, and its charging/discharging voltage scope is 0.01 ~ 3.0V.At 0.1A g
-1its reversible capacity after 100 times that circulates still remains on 285mAh g
-1, its first discharge capacity be 1068mAh g
-1, charging capacity is 756mAh g
-1.
Comparative example 1, made into poly(ethylene oxide) (PEO) (mole is constant) by polyvinylpyrrolidone, all the other are equal to embodiment 1.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test: at 0.1A g
-1its reversible capacity after 100 times that circulates is 340mAh g
-1, its first discharge capacity be 1064mAh g
-1, charging capacity is 762mAh g
-1.
Comparative example 2-1, make the consumption in embodiment 1 into 0.00003mol by polyvinylpyrrolidone 0.00006mol, all the other are equal to embodiment 1.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test: at 0.1A g
-1its reversible capacity after 100 times that circulates is 230mAh g
-1, its first discharge capacity be 982mAhg
-1, charging capacity is 763mAh g
-1.
Comparative example 2-2, make the consumption in embodiment 1 into 0.00015mol by polyvinylpyrrolidone 0.00006mol, all the other are equal to embodiment 1.
By obtained, iron oxide material--iron oxide microballoon negative material carries out being assembled into button cell as method described in experiment 1 and carries out electro-chemical test: at 0.1A g
-1its reversible capacity after 100 times that circulates is 315mAh g
-1, its first discharge capacity be 1002mAh g
-1, charging capacity is 789mAh g
-1.
Finally, it is also to be noted that what enumerate above is only several specific embodiments of the present invention.Obviously, the invention is not restricted to above embodiment, many distortion can also be had.All distortion that those of ordinary skill in the art can directly derive from content disclosed by the invention or associate, all should think protection scope of the present invention.
Claims (3)
1. the preparation method of lithium ion battery iron oxide microballoon negative material, is characterized in that comprising the following steps:
1), by iron salt dissolved in deionized water, iron salt solutions is obtained; Described deionized water and Fe
3+mol ratio be 50 ~ 80:1;
2), to step 1) add acid, described acid and Fe in the iron salt solutions of gained
3+mol ratio be 0.3 ~ 1.0:1; Then add polyvinylpyrrolidone to stir, until polyvinylpyrrolidone dissolves completely; Described polyvinylpyrrolidone and Fe
3+mol ratio be 0.005 ~ 0.015:1;
3), with vigorous stirring add formamide, stir 5 ~ 10 minutes, described formamide and Fe
3+mol ratio be 4 ~ 10:1; Then at 50 ~ 70 DEG C, aged gel is carried out; The aged gel time is 2 ~ 3 hours;
4), by step 3) gel of gained at normal pressure 50 ~ 70 DEG C dry 24 hours, obtain precursor product;
5), by step 4) precursor product of gained is warming up to 500 ~ 800 DEG C of insulations 4 ~ 6 hours in air atmosphere, and be cooled to room temperature, obtain iron oxide microballoon negative material.
2. the preparation method of lithium ion battery iron oxide microballoon negative material according to claim 1, is characterized in that:
Described molysite is high iron chloride; Described acid is hydrochloric acid.
3. the preparation method of lithium ion battery iron oxide microballoon negative material according to claim 2, is characterized in that:
Described deionized water and Fe
3+mol ratio be 50 ~ 60:1, hydrochloric acid and Fe
3+mol ratio be 0.3 ~ 0.4:1, polyvinylpyrrolidone and Fe
3+mol ratio be 0.007 ~ 0.008:1; Formamide and Fe
3+mol ratio be 5.5:1;
Described step 5) in: be warming up to 500 DEG C of insulations 4 hours.
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| CN110112395A (en) * | 2019-05-21 | 2019-08-09 | 东北大学 | A method of iron-based negative electrode material is prepared based on sol-gal process |
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| CN110112395A (en) * | 2019-05-21 | 2019-08-09 | 东北大学 | A method of iron-based negative electrode material is prepared based on sol-gal process |
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